Hybridized surface lattice modes in intercalated 3-disk plasmonic crystals for high figure-of-merit plasmonic sensing

Hybridized surface lattice mode in an intercalated 3-disk plasmonic lattice for overcoming an inherent trade-off in plasmonic sensing.

Multipole and multimode engineering in Mie resonance-based metastructures

Benefited from the well-known Mie resonance, a plethora of physical phenomena and applications are attracting attention in current research on dielectric-based nanophotonics. High-index dielectric metastructures are favorable to enhance light-matter interaction in nanoscale with advantages such as low loss, optical magnetism, and multipolar responses, which are superior to their plasmonic counterpart. In this review, we highlight the important role played by Mie resonance-based multipolar and multimodal interaction in nanophotonics, introducing the concept of “multipole and multimode engineering” in artificially engineered dielectric-based metastructures and providing an overview of the recent progress of this fast-developing area. The scope of multipole and multimode engineering is restricted not only in multipolar interferences of meta-atom and meta-molecule but also in the nontrivial intermodal coupling (Fano resonance and bound states in the continuum), in the collective mode and the surface lattice mode appearing via periodic meta-lattices and aperiodic meta-assembly, in chiral enhancement via chiral and achiral dielectric metastructures, and in Mie resonance-mediated hybrid structures (Mie-plasmon and Mie-exciton). Detailed examples and the underlying physics of this area are discussed in-depth, in order to lead the multifunctional metastructures for novel applications in the future.

High-pressure polymorphism in pyridine

Single crystals of the high-pressure phases II and III of pyridine have been obtained by in situ crystallization at 1.09 and 1.69 GPa, revealing the crystal structure of phase III for the first time using X-ray diffraction. Phase II crystallizes in P212121 with Z′ = 1 and phase III in P41212 with Z′ = ½. Neutron powder diffraction experiments using pyridine-d5 establish approximate equations of state of both phases. The space group and unit-cell dimensions of phase III are similar to the structures of other simple compounds with C 2v molecular symmetry, and the phase becomes stable at high pressure because it is topologically close-packed, resulting in a lower molar volume than the topologically body-centred cubic phase II. Phases II and III have been observed previously by Raman spectroscopy, but have been mis-identified or inconsistently named. Raman spectra collected on the same samples as used in the X-ray experiments establish the vibrational characteristics of both phases unambiguously. The pyridine molecules interact in both phases through CH...π and CH...N interactions. The nature of individual contacts is preserved through the phase transition between phases III and II, which occurs on decompression. A combination of rigid-body symmetry mode analysis and density functional theory calculations enables the soft vibrational lattice mode which governs the transformation to be identified.

Spatially defined molecular emitters coupled to plasmonic nanoparticle arrays

This paper describes how metal–organic frameworks (MOFs) conformally coated on plasmonic nanoparticle arrays can support exciton–plasmon modes with features resembling strong coupling but that are better understood by a weak coupling model. Thin films of Zn-porphyrin MOFs were assembled by dip coating on arrays of silver nanoparticles (NP@MOF) that sustain surface lattice resonances (SLRs). Coupling of excitons with these lattice plasmons led to an SLR-like mixed mode in both transmission and transient absorption spectra. The spectral position of the mixed mode could be tailored by detuning the SLR in different refractive index environments and by changing the periodicity of the nanoparticle array. Photoluminescence showed mode splitting that can be interpreted as modulation of the exciton line shape by the Fano profile of the surface lattice mode, without requiring Rabi splitting. Compared with pristine Zn-porphyrin, hybrid NP@MOF structures achieved a 16-fold enhancement in emission intensity. Our results establish MOFs as a crystalline molecular emitter material that can couple with plasmonic structures for energy exchange and transfer.